Alldinger I, Schaefer K L, Goedde D, Ottaviano L, Dirksen U, Ranft A, Juergens H, Gabbert H E, Knoefel W T, Poremba C
Department of General, Visceral and Pediatric Surgery, Heinrich-Heine-University of Düsseldorf, Düsseldorf, Germany.
J Cancer Res Clin Oncol. 2007 Oct;133(10):749-59. doi: 10.1007/s00432-007-0220-2. Epub 2007 May 25.
Only few clinical factors predict the prognosis of patients with Ewing tumors. Unfavorable outcome is associated with primary metastatic disease, age > 15 years, tumor volume above 200 ml, and the histological response to chemotherapy. The aim of this study was to elucidate the prevalence and clinical impact of microsatellite instability (MSI) together with the relation between MSI and mismatch repair protein expression in Ewing tumors. DNA from 61 primary Ewing tumors and 11 Ewing tumor cell lines was extracted and microsatellite analysis for the detection of instability or loss of heterozygosity was performed for the five markers of the Bethesda panel BAT25, BAT26, D5S346, D2S123, and D17S250, which represents the established marker panel for the analysis of hereditary non-polyposis colorectal carcinoma (HNPCC) patients. In addition, single nucleotide repeat regions of the two tumor genes BAX and transforming growth factor receptor II (TGFBR2) were also included. All of the 61 samples were suitable for LOH analysis and 55 for the determination of MSI-status. LOH of these microsatellite markers was detected in 9 of the 61 patients (14.8%). Over all, genetic instability, i.e. MSI and/or LOH, was detected in 17 tumors (27.9%). One out of the 11 tumor cell lines (STA ET1) was characterized by instability of all the five Bethesda markers, while from primary tumor samples, only one showed MSI in more than one microsatellite marker (D5S346 and D17S250, MSI-high). Eight of the fifty-five patients (14.5%) showed instability of one microsatellite locus (MSI-low). No instability was detected in BAT26, D2S123, BAX and TGFBR2. There was no significant correlation between MSI and loss of expression of mismatch repair proteins MLH1, MSH2, or MSH6. The impairment of the p53 signaling pathway (expression of TP53 and/or MDM2 by immunohistochemistry) was significantly associated with reduced overall survival (15 of 49 patients (30.6%), P = 0.0410, log-rank test). We conclude that MSI is not prevalent in Ewing tumor and that the nature of instability differs from the form observed in colorectal carcinoma, the model tumor of MSI. This is documented by the different pattern of MSI (no BAT26 instability) in Ewing tumors and the lack of a strict correlation between MSI-high and loss of expression of MSH2, MSH6 and MLH1.
仅有少数临床因素可预测尤因肿瘤患者的预后。不良预后与原发性转移性疾病、年龄>15岁、肿瘤体积超过200 ml以及对化疗的组织学反应相关。本研究的目的是阐明微卫星不稳定性(MSI)的患病率和临床影响,以及MSI与尤因肿瘤中错配修复蛋白表达之间的关系。提取了61例原发性尤因肿瘤和11例尤因肿瘤细胞系的DNA,并对贝塞斯达检测板的五个标志物BAT25、BAT26、D5S346、D2S123和D17S250进行微卫星分析,以检测不稳定性或杂合性缺失,这五个标志物代表了用于分析遗传性非息肉病性结直肠癌(HNPCC)患者的既定检测板。此外,还纳入了两个肿瘤基因BAX和转化生长因子受体II(TGFBR2)的单核苷酸重复区域。61个样本均适用于杂合性缺失分析,55个样本适用于MSI状态的测定。在61例患者中的9例(14.8%)检测到这些微卫星标志物的杂合性缺失。总体而言,在17个肿瘤(27.9%)中检测到基因不稳定性,即MSI和/或杂合性缺失。11个肿瘤细胞系中的1个(STA ET1)表现为所有五个贝塞斯达标志物均不稳定,而在原发性肿瘤样本中,只有1个在多个微卫星标志物(D5S346和D17S250,MSI高)中显示MSI。55例患者中的8例(14.5%)表现为一个微卫星位点不稳定(MSI低)。在BAT26、D2S123、BAX和TGFBR2中未检测到不稳定性。MSI与错配修复蛋白MLH1、MSH2或MSH6表达缺失之间无显著相关性。p53信号通路的损害(通过免疫组织化学检测TP53和/或MDM2的表达)与总生存期缩短显著相关(49例患者中的15例(30.6%),P = 0.0410,对数秩检验)。我们得出结论,MSI在尤因肿瘤中并不普遍,且不稳定性的性质与MSI的典型肿瘤结直肠癌中观察到的形式不同。尤因肿瘤中MSI的不同模式(无BAT26不稳定性)以及MSI高与MSH2、MSH6和MLH1表达缺失之间缺乏严格相关性证明了这一点。